Efficacy of Levobupivacaine Versus Levobupivacaine Plus Dexmedetomidine Infiltration for Post-Tonsillectomy Analgesia: A Randomized Controlled Trial.

IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pain Research & Management Pub Date : 2022-09-19 eCollection Date: 2022-01-01 DOI:10.1155/2022/9958668
Ghada Mohammad Abo Elfadl, Marwa Mahmoud AbdelRady, Hany M Osman, Mohamed Omar Gad, Nessren M Abd El-Rady, Wesam Nashat Ali
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引用次数: 1

Abstract

Background: The study evaluated the analgesic effects of levobupivacaine infiltration in the tonsil bed, and a combination of levobupivacaine and dexmedetomidine in patients undergoing tonsillectomy.

Methods: Ninety children (ages 3 to 7 years) who were scheduled for a tonsillectomy were allocated randomly into two groups. (L Group): peritonsillar infiltration with 0.25% levobupivacaine (2 ml + 0.5 ml saline 0.9% per tonsil). (LD Group): levobupivacaine 0.25% (2 ml) plus dexmedetomidine 1 μg/kg diluted in 1 ml saline 0.9% (0.5 ml in each tonsil), and administered by peritonsillar infiltration (2.5 ml per tonsil) following intubation 3-5 minutes before operation. To avoid bias, infiltrate a total volume of 2.5 ml in each tonsil. The first analgesic request time was the primary outcome, with postoperative pain score, total analgesic consumption, total oral intake, sedation, and side effects as secondary outcomes.

Results: The first rescue analgesia time in the LD group was longer (644.31 ± 112.89 min) than in the L group (551.51 ± 146.16 min, P-value <0.001). The number of patients who required >1 analgesic dose in the L group (n = 13) was higher than in the LD group (n = 5). The LD group consumes a lower total dose of IV paracetamol in the first 24 hours postoperatively (321.89 ± 93.25 mg) than the L group (394.89 ± 183.71 mg, P < 0.00-value < 0.050). On the first day postoperatively, patients in the LD group had a higher total oral intake (P < 0.001). Except for a slight increase in laryngospasm in the L group, there were no side effects.

Conclusions: The Children's peritonsillar infiltration of levobupivacaine and dexmedetomidine improved postoperative pain after adenotonsillectomy. The topically applied levobupivacaine and dexmedetomidine were concomitant with no systemic effects, greater total oral intake on the first day postoperative, and higher family satisfaction.

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左旋布比卡因与左旋布比卡因联合右美托咪定浸润治疗扁桃体切除术后镇痛的疗效:一项随机对照试验。
背景:本研究评价左旋布比卡因浸润扁桃体床及左旋布比卡因联合右美托咪定在扁桃体切除术患者中的镇痛作用。方法:90例3 ~ 7岁拟行扁桃体切除术的儿童随机分为两组。(L组):0.25%左布比卡因(2 ml + 0.5 ml生理盐水0.9% /扁桃体)囊周浸润。(LD组):左布比卡因0.25% (2 ml)加右美托咪定1 μg/kg稀释于1 ml 0.9%生理盐水中(每扁桃体0.5 ml),术前3-5分钟插管后经扁桃体周围浸润(每扁桃体2.5 ml)给药。为避免偏误,每个扁桃体浸润总量为2.5 ml。首次使用镇痛药时间是主要结局,术后疼痛评分、镇痛药总用量、口服总摄入量、镇静作用和副作用是次要结局。结果:LD组首次抢救镇痛时间(644.31±112.89 min)长于L组(551.51±146.16 min), p值1镇痛剂量(n = 13)高于LD组(n = 5)。LD组术后24 h静脉注射扑热息痛总剂量(321.89±93.25 mg)低于L组(394.89±183.71 mg, P < 0.000 -value < 0.050)。术后第一天,LD组患者的总口服摄入量较高(P < 0.001)。除L组喉痉挛轻微加重外,无其他副作用。结论:左布比卡因和右美托咪定对儿童腺扁桃体切除术后疼痛有改善作用。局部应用左布比卡因和右美托咪定同时使用,无全身效应,术后第一天总口服摄入量较大,家庭满意度较高。
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来源期刊
Pain Research & Management
Pain Research & Management CLINICAL NEUROLOGY-
CiteScore
5.30
自引率
0.00%
发文量
109
审稿时长
>12 weeks
期刊介绍: Pain Research and Management is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of pain management. The most recent Impact Factor for Pain Research and Management is 1.685 according to the 2015 Journal Citation Reports released by Thomson Reuters in 2016.
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